多硫化物
材料科学
钼
锂(药物)
催化作用
硫黄
电化学
硼
二硫化钼
化学工程
电极
纳米技术
无机化学
化学
复合材料
有机化学
冶金
电解质
物理化学
内分泌学
工程类
医学
作者
Rong Wu,Huakai Xu,Yuwei Zhao,Chenyang Zha,Jun Deng,Chengyu Zhang,Gang Lü,Tianshi Qin,Wei Wang,Yao Yin,Chao Zhu,Lin Wang,Gang Ouyang,Wei Huang
标识
DOI:10.1016/j.ensm.2020.07.040
摘要
High-performance lithium-sulfur batteries are limited by the severe “shuttle effect” of polysulfide migration. To entrap and immobilize polysulfides, the development of catalytic material is an effective strategy for improving the lithium-sulfur batteries. Herein, we demonstrate that borophene-like boron subunits-inserted molybdenum frameworks of molybdenum diboride (MoB2) serves as a polysulfide-anchoring center to power redox reaction processing under the high-efficient electron transfer conditions. Specifically, MoB2 not only offers active sites to anchor polysulfide via covalent B-B and metallic Mo-Mo bonds-based low lithiation structure, but also provides a high conductivity to accelerate polysulfide conversion kinetics. With these advances, the liquid Li2S6-based MoB2 electrode (area: 2 cm2) offers a high initial capacity of 1116 mAh/g, and holds 558 mAh/g at 2 C after 500 cycles. Furthermore, the currently proposed MoB2 catalyst may significantly propel the advancement of electrocatalysis technology from lithium-sulfur batteries to metal-air batteries and carbon dioxide/nitrogen electrochemical reduction.
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